{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Sunnyvale",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78832",
      "recalling_firm": "Hologic, Inc.",
      "address_1": "1240 Elko Dr",
      "address_2": "N/A",
      "postal_code": "94089-2212",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "United States (US), Guam (GU), Japan (JP)",
      "recall_number": "Z-0677-2018",
      "product_description": "Rapid for the TLiIQ(R) System, HOLOGIC(R), Catalog number: 01200Q",
      "product_quantity": "N/A",
      "reason_for_recall": "Rapid fFN cassettes were manufactured with material (A137 ascites) from a new supplier (SDIX). The products were distributed to customers before FDA approved the change to use the material from SDIX.",
      "recall_initiation_date": "20171129",
      "center_classification_date": "20180221",
      "termination_date": "20180822",
      "report_date": "20180228",
      "code_info": "E7058"
    }
  ]
}